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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1354017Erstellt: 25. Oktober 2026

Diisopropylethylamine → HCID 10110214, Verbindung

https://huagongshe.com/reaction/1354017

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt3'-Methyl-biphenyl-4-carboxylic acidHCID 2759816—
Edukt10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a][1,4]diazepineHCID 15547048—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelThionyl ChlorideHCID 24386—
ProduktHCID 10110214HCID 1011021482,9%

Reaktionsschritte

A suspension of 3′-methyl-[1,1′-biphenyl]-4-carboxylic acid of Step B (0.50 g, 2.36 mmol) in thionyl chloride (3 mL) was heated at reflux for 30 minutes. After cooling, the thionyl chloride was removed in vacuo. The residue was dissolved in toluene and concentrated in vacuo to give the crude acid chloride as a yellow oil. The acid chloride was then dissolved in dichloromethane (5 mL) and slowly added to a solution of the 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine (0.65 g, 3.53 mmol) and N,N-diisopropylethyl amine (0.90 mL, 5.17 mmol) in dichloromethane (15 mL). After stirring for 2 hours, the reaction was quenched with water. The organic layer was washed with 1 N hydrochloric acid, 1 N sodium hydroxide and brine, dried over anhydrous sodium sulfate, and concentrated in vacuo to give a white foam. Purification of the residue by flash chromatography using a solvent gradient from 15% to 25% of ethyl acetate in hexane gave a white foam which was crystallized by sonication from ethyl acetate/hexane to provide the title compound (0.74 g, 82.8%) as a white solid, m.p. 128–130° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07223752B2
Quelldatensatzuspto-grants-2007_05
ORD IDord-4741ca4e0b264faeab126c3eb69a8f40
Quellennotizuspto-grants-2007_05